FDA 510(k) Application Details - K202197

Device Classification Name	System, Thermal Regulating   More FDA Info for this Device
510(K) Number	K202197
Device Name	System, Thermal Regulating
Applicant	Stihler Electronic GmbH Julius-Hoelder-Strasse 36 Stuttgart 70597 DE Other 510(k) Applications for this Company
Contact	Jens- Peter Weege Other 510(k) Applications for this Contact
Regulation Number	870.5900   More FDA Info for this Regulation Number
Classification Product Code	DWJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/05/2020
Decision Date	09/04/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review